Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Roberto Giugliani

Showing results (61-70 of 482) with videos related to

Pageof 49
Sort By:
Orphanet Journal of Rare Diseases|October 5, 2017
Clinical outcomes in idursulfase-treated patients with mucopolysaccharidosis type II: 3-year data from the hunter outcome survey (HOS)Joseph Muenzer, Roberto Giugliani, Maurizio Scarpa, et al.
Journal of the American College of Nutrition|February 19, 2014
Anthropometry, nutritional status, and dietary intake in pediatric patients with osteogenesis imperfectaMarina B Zambrano, Evelise S Brizola, Lilia Refosco, et al.
Heart and Vessels|August 24, 2018
Aortic root dilatation in patients with mucopolysaccharidoses and the impact of enzyme replacement therapyFabiano de Oliveira Poswar, Carolina Fischinger Moura de Souza, Roberto Giugliani, et al.
Molecular Genetics and Metabolism|February 6, 2016
The natural history of growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS)Rossella Parini, Simon A Jones, Paul R Harmatz, et al.
Therapeutics and Clinical Risk Management|December 29, 2022
Diagnosis and Emerging Treatment Strategies for Mucopolysaccharidosis VII (Sly Syndrome)Fabiano de Oliveira Poswar, Johanna Henriques Nehm, Francyne Kubaski, et al.
American Journal of Medical Genetics. Part A|December 7, 2017
Intrafamilial variability in the clinical manifestations of mucopolysaccharidosis type II: Data from the Hunter Outcome Survey (HOS)Can Ficicioglu, Roberto Giugliani, Paul Harmatz, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie|May 12, 2009
Alpha-mannosidase activity in goats fed with Sida carpinifoliaMarisete Bedin, Edson Moleta Colodel, Marli Viapiana, et al.
Journal of Community Genetics|May 14, 2025
Clinical research in rare diseases in Brazil: challenges and opportunitiesLarissa Pozzebon da Silva, Taiane Alves Vieira, Gabriela Leiria da Silveira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Initial report from the Hunter Outcome SurveyJ Edmond Wraith, Michael Beck, Roberto Giugliani, et al.
Neuroimaging Clinics of North America|December 6, 2014
Brain imaging and genetic risk in the pediatric population, part 1: inherited metabolic diseasesMaria Gabriela Longo, Filippo Vairo, Carolina Fischinger Souza, et al.
Pageof 49

Showing results (61-70 of 482) with videos related to

Sort By:
Pageof 49
Orphanet Journal of Rare Diseases|October 5, 2017
Clinical outcomes in idursulfase-treated patients with mucopolysaccharidosis type II: 3-year data from the hunter outcome survey (HOS)Joseph Muenzer, Roberto Giugliani, Maurizio Scarpa, et al.
Journal of the American College of Nutrition|February 19, 2014
Anthropometry, nutritional status, and dietary intake in pediatric patients with osteogenesis imperfectaMarina B Zambrano, Evelise S Brizola, Lilia Refosco, et al.
Heart and Vessels|August 24, 2018
Aortic root dilatation in patients with mucopolysaccharidoses and the impact of enzyme replacement therapyFabiano de Oliveira Poswar, Carolina Fischinger Moura de Souza, Roberto Giugliani, et al.
Molecular Genetics and Metabolism|February 6, 2016
The natural history of growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS)Rossella Parini, Simon A Jones, Paul R Harmatz, et al.
Therapeutics and Clinical Risk Management|December 29, 2022
Diagnosis and Emerging Treatment Strategies for Mucopolysaccharidosis VII (Sly Syndrome)Fabiano de Oliveira Poswar, Johanna Henriques Nehm, Francyne Kubaski, et al.
American Journal of Medical Genetics. Part A|December 7, 2017
Intrafamilial variability in the clinical manifestations of mucopolysaccharidosis type II: Data from the Hunter Outcome Survey (HOS)Can Ficicioglu, Roberto Giugliani, Paul Harmatz, et al.
Experimental and Toxicologic Pathology : Official Journal of the Gesellschaft Fur Toxikologische Pathologie|May 12, 2009
Alpha-mannosidase activity in goats fed with Sida carpinifoliaMarisete Bedin, Edson Moleta Colodel, Marli Viapiana, et al.
Journal of Community Genetics|May 14, 2025
Clinical research in rare diseases in Brazil: challenges and opportunitiesLarissa Pozzebon da Silva, Taiane Alves Vieira, Gabriela Leiria da Silveira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 27, 2008
Initial report from the Hunter Outcome SurveyJ Edmond Wraith, Michael Beck, Roberto Giugliani, et al.
Neuroimaging Clinics of North America|December 6, 2014
Brain imaging and genetic risk in the pediatric population, part 1: inherited metabolic diseasesMaria Gabriela Longo, Filippo Vairo, Carolina Fischinger Souza, et al.
Pageof 49